Variant report

Variant	rs148786174
Chromosome Location	chr4:3486618-3486619
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	MYC	chr4:3485851-3486788	MCF10A-Er-Src	breast:	n/a	chr4:3486012-3486021
2	ZBTB7A	chr4:3484964-3488054	ECC-1	luminal epithelium:	n/a	chr4:3485633-3485641
3	FOXM1	chr4:3484986-3487210	ECC-1	luminal epithelium:	n/a	n/a
4	EBF1	chr4:3486210-3487261	GM12878	blood:	n/a	chr4:3487022-3487032 chr4:3487039-3487050 chr4:3487022-3487031 chr4:3487021-3487032 chr4:3487022-3487031 chr4:3487020-3487033
5	EP300	chr4:3485064-3487144	ECC-1	luminal epithelium:	n/a	chr4:3485583-3485599
6	SRF	chr4:3485576-3486995	ECC-1	luminal epithelium:	n/a	n/a
7	CREB1	chr4:3485896-3486689	ECC-1	luminal epithelium:	n/a	n/a
8	TCF12	chr4:3486163-3487219	MCF-7	breast:	n/a	n/a
9	SRF	chr4:3485799-3487119	ECC-1	luminal epithelium:	n/a	n/a
10	MAX	chr4:3485579-3487154	MCF-7	breast:	n/a	chr4:3486892-3486902 chr4:3486927-3486937 chr4:3486012-3486021
11	FOXA1	chr4:3486416-3486708	ECC-1	luminal epithelium:	n/a	n/a
12	NR3C1	chr4:3485854-3487027	ECC-1	luminal epithelium:	n/a	n/a
13	ESR1	chr4:3485740-3487450	ECC-1	luminal epithelium:	n/a	n/a
14	POLR2A	chr4:3486198-3486635	ProgFib	skin:	n/a	n/a
15	GABPA	chr4:3486345-3487564	MCF-7	breast:	n/a	chr4:3486892-3486901
16	EGR1	chr4:3486145-3487153	MCF-7	breast:	n/a	chr4:3486778-3486788 chr4:3486775-3486788 chr4:3486887-3486900
17	TCF7L2	chr4:3486215-3486703	MCF-7	breast:	n/a	n/a
18	CREB1	chr4:3485934-3486768	ECC-1	luminal epithelium:	n/a	n/a
19	RCOR1	chr4:3486185-3486668	Hela-S3	cervix:	n/a	n/a
20	ZBTB7A	chr4:3485033-3487141	ECC-1	luminal epithelium:	n/a	chr4:3485633-3485641
21	FOXA2	chr4:3486327-3486724	A549	lung:	n/a	n/a
22	EP300	chr4:3484927-3487690	ECC-1	luminal epithelium:	n/a	chr4:3485583-3485599
23	GATA3	chr4:3486201-3487205	MCF-7	breast:	n/a	n/a
24	ESR1	chr4:3485860-3486641	ECC-1	luminal epithelium:	n/a	n/a
25	FOS	chr4:3486401-3486697	MCF10A-Er-Src	breast:	n/a	n/a
26	FOXM1	chr4:3485748-3486995	ECC-1	luminal epithelium:	n/a	n/a
27	FOXM1	chr4:3486160-3487130	MCF-7	breast:	n/a	n/a
28	FOXA1	chr4:3486437-3486686	ECC-1	luminal epithelium:	n/a	n/a
29	REST	chr4:3485929-3486719	ECC-1	luminal epithelium:	n/a	n/a
30	GABPA	chr4:3485936-3487689	MCF-7	breast:	n/a	chr4:3486892-3486901
31	MYC	chr4:3485820-3487020	MCF-7	breast:	n/a	chr4:3486892-3486902 chr4:3486927-3486937 chr4:3486012-3486021
32	ESR1	chr4:3485819-3487513	ECC-1	luminal epithelium:	n/a	n/a
33	RAD21	chr4:3485776-3486871	ECC-1	luminal epithelium:	n/a	chr4:3486675-3486687
34	JUND	chr4:3486198-3487156	MCF-7	breast:	n/a	chr4:3486980-3486991
35	TCF12	chr4:3485783-3487617	MCF-7	breast:	n/a	chr4:3486044-3486052 chr4:3486087-3486097
36	MYC	chr4:3485725-3487081	MCF-7	breast:	n/a	chr4:3486892-3486902 chr4:3486927-3486937 chr4:3486012-3486021
37	HA-E2F1	chr4:3485875-3486910	MCF-7	breast:	n/a	n/a
38	TAF1	chr4:3485867-3486986	ECC-1	luminal epithelium:	n/a	n/a
39	USF1	chr4:3485643-3487087	ECC-1	luminal epithelium:	n/a	n/a
40	EGR1	chr4:3485800-3487135	ECC-1	luminal epithelium:	n/a	chr4:3486778-3486788 chr4:3486775-3486788 chr4:3486887-3486900
41	TCF12	chr4:3484972-3487780	ECC-1	luminal epithelium:	n/a	chr4:3487770-3487780 chr4:3485420-3485427 chr4:3486044-3486052 chr4:3486087-3486097
42	MAX	chr4:3484979-3487596	ECC-1	luminal epithelium:	n/a	chr4:3485249-3485258 chr4:3485250-3485257 chr4:3485248-3485259 chr4:3486892-3486902 chr4:3486927-3486937 chr4:3486012-3486021
43	TCF7L2	chr4:3486313-3486712	Hela-S3	cervix:	n/a	n/a
44	GATA3	chr4:3486238-3486930	MCF-7	breast:	n/a	n/a
45	HDAC2	chr4:3485913-3486819	MCF-7	breast:	n/a	n/a
46	MAX	chr4:3486439-3487557	NB4	blood:	n/a	chr4:3486892-3486902 chr4:3486927-3486937
47	MXI1	chr4:3486365-3486693	Hela-S3	cervix:	n/a	n/a
48	STAT3	chr4:3486384-3486654	MCF10A-Er-Src	breast:	n/a	chr4:3486624-3486636
49	NR2F2	chr4:3485915-3487245	MCF-7	breast:	n/a	n/a
50	EBF1	chr4:3486155-3486625	GM12878	blood:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr4:3418569..3420412-chr4:3484561..3487471,2	MCF-7	breast:
2	chr4:3484714..3487220-chr4:3532599..3535251,4	MCF-7	breast:
3	chr4:3464629..3465770-chr4:3486550..3487347,4	MCF-7	breast:
4	chr4:3292637..3295776-chr4:3483843..3488274,4	MCF-7	breast:
5	chr4:3484197..3487656-chr4:3491883..3496058,4	K562	blood:
6	chr4:3464614..3465179-chr4:3486100..3486697,2	MCF-7	breast:
7	chr4:3485927..3488368-chr4:3533732..3536345,3	MCF-7	breast:
8	chr4:3386285..3389665-chr4:3485168..3487566,3	MCF-7	breast:
9	chr4:3464939..3465859-chr4:3486070..3487026,3	MCF-7	breast:

Variant related genes	Relation type
DOK7	TF binding region
ENSG00000175920	Chromatin interaction
ENSG00000159788	Chromatin interaction
ENSG00000163956	Chromatin interaction

Extended variants
information (count: 57 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:57 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv428106	chr4:3226182-3752322	Enhancers ZNF genes & repeats Weak transcription Strong transcription Active TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
2	nsv878462	chr4:3311548-3505448	Strong transcription Enhancers Weak transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
3	nsv1007847	chr4:3317904-3527357	Enhancers Weak transcription ZNF genes & repeats Genic enhancers Flanking Active TSS Bivalent/Poised TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	13 gene(s)	inside rSNPs	diseases
4	nsv537001	chr4:3317904-3527357	Weak transcription Enhancers Strong transcription Genic enhancers Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	13 gene(s)	inside rSNPs	diseases
5	nsv878463	chr4:3363994-3498896	Enhancers Weak transcription Bivalent Enhancer Strong transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
6	nsv428435	chr4:3386773-3623321	Enhancers Strong transcription Weak transcription Genic enhancers Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases
7	nsv933265	chr4:3392824-4283640	Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	60 gene(s)	inside rSNPs	diseases
8	esv2757918	chr4:3394344-4350986	Enhancers Strong transcription Flanking Active TSS Active TSS Genic enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	64 gene(s)	inside rSNPs	diseases
9	esv2759219	chr4:3394344-4350986	Weak transcription Flanking Active TSS Strong transcription Enhancers Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	64 gene(s)	inside rSNPs	diseases
10	nsv878464	chr4:3405165-3505448	Bivalent Enhancer Weak transcription Enhancers Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Flanking Active TSS ZNF genes & repeats Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
11	nsv878465	chr4:3405165-3566567	Strong transcription Flanking Active TSS Weak transcription Enhancers Active TSS Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
12	esv1791851	chr4:3407753-3534022	Bivalent Enhancer Enhancers Strong transcription Bivalent/Poised TSS Weak transcription Genic enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
13	nsv1000383	chr4:3412585-3839781	Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	30 gene(s)	inside rSNPs	diseases
14	nsv878469	chr4:3413209-3566567	Weak transcription Genic enhancers Active TSS Enhancers Flanking Active TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
15	nsv878470	chr4:3413209-3566567	Weak transcription Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
16	nsv878471	chr4:3413209-3884998	Bivalent Enhancer Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	30 gene(s)	inside rSNPs	diseases
17	esv1816543	chr4:3414654-3942867	Enhancers Bivalent Enhancer Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	35 gene(s)	inside rSNPs	diseases
18	nsv1001328	chr4:3421979-3654381	Bivalent/Poised TSS Enhancers Bivalent Enhancer Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats Weak transcription Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases
19	nsv878474	chr4:3422211-3504562	Weak transcription Bivalent Enhancer Strong transcription Enhancers Active TSS Genic enhancers Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
20	nsv1008575	chr4:3429062-3487322	Bivalent Enhancer Weak transcription Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
21	nsv967719	chr4:3429579-3535969	Genic enhancers Active TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
22	nsv470004	chr4:3429856-3584373	Bivalent Enhancer Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Strong transcription Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
23	nsv878475	chr4:3431342-3504562	Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Enhancers Genic enhancers ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
24	nsv516505	chr4:3434336-3504562	Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer Enhancers Strong transcription Flanking Active TSS Genic enhancers Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
25	nsv1011554	chr4:3436478-3975772	ZNF genes & repeats Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	38 gene(s)	inside rSNPs	diseases
26	nsv537002	chr4:3436478-3975772	Weak transcription Flanking Active TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Active TSS Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	38 gene(s)	inside rSNPs	diseases
27	nsv878476	chr4:3436588-3504562	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
28	nsv878477	chr4:3438643-3584059	ZNF genes & repeats Enhancers Strong transcription Weak transcription Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
29	nsv829840	chr4:3444216-3623031	Genic enhancers Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription Strong transcription ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	24 gene(s)	inside rSNPs	diseases
30	nsv878478	chr4:3447243-3566567	Bivalent Enhancer Active TSS Genic enhancers Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
31	nsv1002774	chr4:3450810-3577017	Enhancers Weak transcription Active TSS Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases
32	nsv1012371	chr4:3450810-3878976	Enhancers Flanking Active TSS Bivalent Enhancer Strong transcription Weak transcription Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	30 gene(s)	inside rSNPs	diseases
33	nsv537003	chr4:3450810-3878976	Active TSS Bivalent Enhancer Enhancers Genic enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	30 gene(s)	inside rSNPs	diseases
34	nsv998670	chr4:3453787-3909535	Active TSS Bivalent Enhancer Strong transcription Flanking Active TSS Enhancers ZNF genes & repeats Weak transcription Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	33 gene(s)	inside rSNPs	diseases
35	nsv878479	chr4:3461900-3498896	Enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Weak transcription Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
36	nsv878480	chr4:3461900-3504562	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Genic enhancers Bivalent/Poised TSS Active TSS Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
37	nsv878481	chr4:3461900-3566567	Strong transcription Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Weak transcription Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
38	nsv878482	chr4:3461900-3573260	Bivalent Enhancer Strong transcription Enhancers Weak transcription Flanking Active TSS Genic enhancers Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
39	nsv878483	chr4:3461900-3683269	Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats Active TSS Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases
40	nsv1008394	chr4:3462618-3577017	Weak transcription Enhancers Strong transcription Bivalent Enhancer Flanking Active TSS Active TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases
41	esv1806490	chr4:3463724-3501161	Strong transcription Weak transcription Enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
42	esv1808609	chr4:3463924-3500961	Bivalent Enhancer Weak transcription Enhancers Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Strong transcription Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
43	nsv461170	chr4:3471754-3496940	Weak transcription Strong transcription Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
44	nsv593458	chr4:3471754-3496940	Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
45	esv2757031	chr4:3472162-3510598	Bivalent Enhancer Strong transcription Weak transcription Enhancers Genic enhancers Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
46	nsv998512	chr4:3472878-3643547	Enhancers Bivalent Enhancer Active TSS Flanking Active TSS Weak transcription ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	24 gene(s)	inside rSNPs	diseases
47	nsv537004	chr4:3472878-3643547	Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats Enhancers Bivalent Enhancer Active TSS Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	24 gene(s)	inside rSNPs	diseases
48	nsv878484	chr4:3473139-3499153	Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Bivalent/Poised TSS Genic enhancers Strong transcription Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
49	nsv878485	chr4:3473139-3525057	Bivalent Enhancer Weak transcription Strong transcription Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
50	nsv878486	chr4:3473139-3573260	Bivalent Enhancer Enhancers Weak transcription Strong transcription Active TSS Genic enhancers Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:88 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:3467000-3493600	Weak transcription	Aorta	Aorta
2	chr4:3476800-3490800	Bivalent Enhancer	Fetal Muscle Trunk	muscle
3	chr4:3481000-3489200	Enhancers	Fetal Heart	heart
4	chr4:3481200-3488800	Enhancers	Left Ventricle	heart
5	chr4:3481400-3491200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
6	chr4:3482400-3487200	Bivalent Enhancer	Fetal Muscle Leg	muscle
7	chr4:3483000-3486800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
8	chr4:3483200-3489600	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
9	chr4:3485000-3486800	Enhancers	Brain Angular Gyrus	brain
10	chr4:3485000-3489400	Bivalent Enhancer	Placenta	Placenta
11	chr4:3485200-3486800	Bivalent Enhancer	H9 Derived Neuron Cultured Cells	ES cell derived
12	chr4:3485200-3486800	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
13	chr4:3485200-3486800	Bivalent Enhancer	Fetal Stomach	stomach
14	chr4:3485200-3487400	Enhancers	Pancreas	Pancrea
15	chr4:3485200-3487400	Bivalent Enhancer	Sigmoid Colon	Sigmoid Colon
16	chr4:3485200-3487400	Enhancers	Spleen	Spleen
17	chr4:3485200-3488200	Flanking Active TSS	HMEC	breast
18	chr4:3485200-3489400	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
19	chr4:3485200-3489600	Bivalent Enhancer	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
20	chr4:3485400-3486800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
21	chr4:3485400-3487600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr4:3485400-3488200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
23	chr4:3485400-3488600	Flanking Active TSS	Primary B cells from peripheral blood	blood
24	chr4:3485400-3489800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr4:3485600-3486800	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
26	chr4:3485600-3486800	Flanking Active TSS	HSMM	muscle
27	chr4:3485600-3487000	Bivalent Enhancer	Fetal Thymus	thymus
28	chr4:3485600-3488000	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
29	chr4:3485600-3488600	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
30	chr4:3485800-3486800	Bivalent Enhancer	ES-WA7 Cell Line	embryonic stem cell
31	chr4:3485800-3486800	Bivalent Enhancer	Brain Substantia Nigra	brain
32	chr4:3485800-3486800	Flanking Active TSS	Osteobl	bone
33	chr4:3485800-3487000	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
34	chr4:3485800-3487000	Bivalent Enhancer	GM12878-XiMat	blood
35	chr4:3485800-3487000	Flanking Bivalent TSS/Enh	NHEK	skin
36	chr4:3485800-3487200	Bivalent Enhancer	Adipose Nuclei	Adipose
37	chr4:3485800-3487600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
38	chr4:3485800-3487600	Flanking Bivalent TSS/Enh	Foreskin Keratinocyte Primary Cells skin02	Skin
39	chr4:3485800-3487600	Flanking Active TSS	Esophagus	oesophagus
40	chr4:3486000-3486800	Bivalent Enhancer	Primary hematopoietic stem cells	blood
41	chr4:3486000-3486800	Bivalent Enhancer	Primary T killer naive cells fromperipheralblood	blood
42	chr4:3486000-3487000	Flanking Active TSS	Hela-S3	cervix
43	chr4:3486000-3487600	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
44	chr4:3486000-3488000	Bivalent Enhancer	Placenta Amnion	Placenta Amnion
45	chr4:3486000-3488200	Flanking Active TSS	Primary Natural Killer cells fromperipheralblood	blood
46	chr4:3486000-3489000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
47	chr4:3486200-3486800	Bivalent Enhancer	Primary mononuclear cells fromperipheralblood	Blood
48	chr4:3486200-3487000	Bivalent Enhancer	Primary T cells effector/memory enriched fromperipheralblood	blood
49	chr4:3486200-3487000	Bivalent Enhancer	Fetal Intestine Large	intestine
50	chr4:3486200-3487000	Bivalent Enhancer	Fetal Intestine Small	intestine

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