Variant report

Variant	rs4974860
Chromosome Location	chr4:9604201-9604202
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:61)
Chromatin interactive
region (count:0)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:9604187-9604237	MCF-7	breast:	n/a
2	chr4:9604187-9604237	NH-A	brain:	n/a
3	chr4:9604187-9604237	SK-N-SH_RA	brain:	n/a
4	chr4:9604187-9604237	Hepatocyte	liver:	n/a
5	chr4:9604187-9604237	AG04450	lung:	fetal
6	chr4:9604187-9604237	NT2-D1	testis:	n/a
7	chr4:9604187-9604237	HPAEpiC	pulmonary alveolar:	n/a
8	chr4:9604187-9604237	Jurkat	blood:	n/a
9	chr4:9604187-9604237	HCPEpiC	choroid plexus:	n/a
10	chr4:9604187-9604237	AG09319	gingival:	n/a
11	chr4:9604187-9604237	Hela-S3	cervix:	n/a
12	chr4:9604187-9604237	HNPCEpiC	eye:	n/a
13	chr4:9604187-9604237	MCF10A-Er-Src	breast:	n/a
14	chr4:9604187-9604237	HEEpiC	esophagus:	n/a
15	chr4:9604187-9604237	GM12891	blood:	n/a
16	chr4:9604187-9604237	GM12892	blood:	n/a
17	chr4:9604187-9604237	PrEC	prostate:	n/a
18	chr4:9604187-9604237	SK-N-MC	brain:	n/a
19	chr4:9604187-9604237	HL-60	blood:	n/a
20	chr4:9604187-9604237	PFSK-1	brain:	n/a
21	chr4:9604187-9604237	HepG2	liver:	n/a
22	chr4:9604187-9604237	RPTEC	kidney:	n/a
23	chr4:9604187-9604237	AG09309	skin:	n/a
24	chr4:9604187-9604237	SKMC	muscle:	n/a
25	chr4:9604187-9604237	HCT-116	colon:	n/a
26	chr4:9604187-9604237	U87	brain:	n/a
27	chr4:9604187-9604237	HCF	heart:	n/a
28	chr4:9604187-9604237	H1-hESC	embryonic stem cell:	embryo
29	chr4:9604187-9604237	CMK	blood:	n/a
30	chr4:9604187-9604237	AoSMC	blood vessel:	n/a
31	chr4:9604187-9604237	SK-N-SH	brain:	n/a
32	chr4:9604187-9604237	K562	blood:	n/a
33	chr4:9604187-9604237	GM06990	blood:	n/a
34	chr4:9604187-9604237	NHBE	bronchial:	n/a
35	chr4:9604187-9604237	HCM	heart:	n/a
36	chr4:9604187-9604237	BJ	skin:	n/a
37	chr4:9604187-9604237	HMEC	breast:	n/a
38	chr4:9604187-9604237	LNCaP	prostate:	n/a
39	chr4:9604187-9604237	HUVEC	blood vessel:	n/a
40	chr4:9604187-9604237	SAEC	small airway:	n/a
41	chr4:9604187-9604237	AG04449	skin:	fetal
42	chr4:9604187-9604237	HRPEpiC	eye:	n/a
43	chr4:9604187-9604237	HRE	kidney:	n/a
44	chr4:9604187-9604237	A549	lung:	n/a
45	chr4:9604187-9604237	BE2_C	brain:	n/a
46	chr4:9604187-9604237	NHDF-neo	bronchial:	n/a
47	chr4:9604187-9604237	ProgFib	skin:	n/a
48	chr4:9604187-9604237	HRCEpiC	kidney:	n/a
49	chr4:9604187-9604237	NB4	blood:	n/a
50	chr4:9604187-9604237	GM19239	blood:	n/a

No data

Variant related genes	Relation type
ENSG00000265901	CpG island

Extended variants
information (count: 99 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:55)

rs_ID	r²[population]
rs10000206	0.83[AFR][1000 genomes];0.82[AMR][1000 genomes];0.82[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10007322	0.93[AFR][1000 genomes];0.88[AMR][1000 genomes];0.82[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10939395	0.83[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs10939406	0.99[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10939407	0.90[AFR][1000 genomes];0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10939410	0.87[AFR][1000 genomes];0.88[AMR][1000 genomes];0.84[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10939411	0.98[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10939413	0.97[AFR][1000 genomes];0.84[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11736694	0.97[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11737872	0.86[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12648085	0.82[EUR][1000 genomes]
rs13118016	0.92[EUR][1000 genomes]
rs13118208	0.92[EUR][1000 genomes]
rs13131693	0.82[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs13152842	1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1809400	0.91[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1809401	0.93[AFR][1000 genomes];0.94[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1842489	0.97[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1871717	0.82[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1871718	0.82[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1871720	0.91[ASN][1000 genomes]
rs1966999	0.92[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1967000	1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2004333	0.83[AFR][1000 genomes];0.82[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2004334	0.89[AFR][1000 genomes];0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2046112	1.00[EUR][1000 genomes]
rs2086430	1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2101074	1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs35722426	0.82[EUR][1000 genomes]
rs4404541	0.83[AFR][1000 genomes];0.90[ASN][1000 genomes]
rs4974813	0.87[ASN][1000 genomes]
rs4974817	0.87[AFR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4974820	0.93[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4974821	0.97[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4974822	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4974852	0.82[AFR][1000 genomes];0.82[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4974855	0.92[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4974857	0.98[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs57504588	0.82[EUR][1000 genomes]
rs6448855	0.82[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6814674	0.82[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6815282	0.98[ASN][1000 genomes]
rs6816115	1.00[EUR][1000 genomes]
rs6820385	0.87[AFR][1000 genomes]
rs6842111	0.93[AFR][1000 genomes];0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6849083	0.98[AFR][1000 genomes];0.94[AMR][1000 genomes];0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6855150	0.95[AFR][1000 genomes];0.99[ASN][1000 genomes]
rs6855527	0.82[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs734628	0.89[AFR][1000 genomes];0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7439897	0.82[EUR][1000 genomes]
rs7672393	0.82[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9291586	0.98[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs9684038	0.92[EUR][1000 genomes]
rs9917942	0.85[AFR][1000 genomes];0.82[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9993066	0.94[AFR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:44 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv878634	chr4:8729638-9609506	Enhancers Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Active TSS Weak transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	64 gene(s)	inside rSNPs	diseases
2	nsv878635	chr4:8729638-9614926	Bivalent Enhancer Weak transcription Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Flanking Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	64 gene(s)	inside rSNPs	diseases
3	nsv878636	chr4:8729638-9626304	Active TSS ZNF genes & repeats Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription Strong transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	64 gene(s)	inside rSNPs	diseases
4	nsv878637	chr4:8729638-9651413	Flanking Bivalent TSS/Enh Enhancers Weak transcription Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	64 gene(s)	inside rSNPs	diseases
5	nsv878638	chr4:8729638-9687969	Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	66 gene(s)	inside rSNPs	diseases
6	esv1796218	chr4:9324644-9714338	Enhancers Active TSS Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription ZNF genes & repeats Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	32 gene(s)	inside rSNPs	diseases
7	nsv428108	chr4:9324644-9764173	Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Weak transcription ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	35 gene(s)	inside rSNPs	diseases
8	nsv998504	chr4:9370690-9632436	Enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Active TSS Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA	17 gene(s)	inside rSNPs	diseases
9	nsv1002765	chr4:9370690-9633990	Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS Enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA	17 gene(s)	inside rSNPs	diseases
10	nsv1006342	chr4:9370690-9678661	Weak transcription Flanking Active TSS Enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	18 gene(s)	inside rSNPs	diseases
11	nsv533218	chr4:9371016-10252290	Active TSS Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	74 gene(s)	inside rSNPs	diseases
12	nsv818213	chr4:9371116-9719981	Active TSS Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers Bivalent/Poised TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA	22 gene(s)	inside rSNPs	diseases
13	esv2754610	chr4:9372303-9804524	Enhancers Active TSS Bivalent/Poised TSS Weak transcription Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA	28 gene(s)	inside rSNPs	diseases
14	nsv999172	chr4:9376566-9633990	Enhancers Flanking Bivalent TSS/Enh Active TSS Weak transcription Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Flanking Active TSS Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	17 gene(s)	inside rSNPs	diseases
15	nsv432575	chr4:9381818-9609115	Enhancers Bivalent/Poised TSS Active TSS Bivalent Enhancer Weak transcription Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA	17 gene(s)	inside rSNPs	diseases
16	nsv997355	chr4:9381818-9615079	Active TSS Weak transcription Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA	17 gene(s)	inside rSNPs	diseases
17	esv1837127	chr4:9381818-9681650	Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	18 gene(s)	inside rSNPs	diseases
18	nsv530090	chr4:9383695-10165033	Enhancers Genic enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	70 gene(s)	inside rSNPs	diseases
19	nsv878655	chr4:9384748-9609506	Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Weak transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA	17 gene(s)	inside rSNPs	diseases
20	nsv1012865	chr4:9429299-9794181	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	23 gene(s)	inside rSNPs	diseases
21	nsv1001143	chr4:9435322-9794181	Active TSS Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA	23 gene(s)	inside rSNPs	diseases
22	nsv999615	chr4:9436994-9615079	Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	13 gene(s)	inside rSNPs	diseases
23	nsv1011425	chr4:9436994-9715105	Weak transcription Flanking Active TSS Bivalent Enhancer Enhancers Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	18 gene(s)	inside rSNPs	diseases
24	nsv508273	chr4:9442862-9636380	Active TSS Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Bivalent/Poised TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA	13 gene(s)	inside rSNPs	diseases
25	nsv1002981	chr4:9446035-9698645	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	16 gene(s)	inside rSNPs	diseases
26	nsv1007204	chr4:9456977-9707068	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	16 gene(s)	inside rSNPs	diseases
27	nsv1006867	chr4:9456977-9713612	Active TSS Enhancers Flanking Active TSS Weak transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	17 gene(s)	inside rSNPs	diseases
28	nsv1002757	chr4:9456977-9715105	Flanking Bivalent TSS/Enh Active TSS Enhancers Bivalent/Poised TSS Weak transcription Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	17 gene(s)	inside rSNPs	diseases
29	nsv1012621	chr4:9456977-9802366	Flanking Active TSS Weak transcription Enhancers Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	23 gene(s)	inside rSNPs	diseases
30	nsv1012965	chr4:9461218-9696765	Flanking Active TSS Active TSS Weak transcription Strong transcription Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	14 gene(s)	inside rSNPs	diseases
31	nsv1012634	chr4:9461218-9802366	Flanking Active TSS Enhancers Weak transcription Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	22 gene(s)	inside rSNPs	diseases
32	nsv878665	chr4:9470222-9651413	Flanking Active TSS Enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS Weak transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	11 gene(s)	inside rSNPs	diseases
33	nsv878666	chr4:9486579-9626304	Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	8 gene(s)	inside rSNPs	diseases
34	nsv1013387	chr4:9496282-9633990	Active TSS Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	7 gene(s)	inside rSNPs	diseases
35	nsv1000308	chr4:9496282-9674336	Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	8 gene(s)	inside rSNPs	diseases
36	nsv998043	chr4:9496282-9830208	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Strong transcription Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	18 gene(s)	inside rSNPs	diseases
37	esv10795	chr4:9508396-9745703	Weak transcription Active TSS Enhancers Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA	13 gene(s)	inside rSNPs	diseases
38	nsv980183	chr4:9514318-9619185	Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	7 gene(s)	inside rSNPs	diseases
39	nsv878667	chr4:9543673-9903121	ZNF genes & repeats Active TSS Enhancers Weak transcription Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	16 gene(s)	inside rSNPs	diseases
40	nsv520290	chr4:9551094-9626409	Enhancers ZNF genes & repeats Active TSS Weak transcription Flanking Active TSS Genic enhancers Bivalent Enhancer Strong transcription	TF binding region CpG island lncRNA miRNA	5 gene(s)	inside rSNPs	diseases
41	nsv878668	chr4:9551094-9651413	Enhancers Active TSS Flanking Active TSS Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Bivalent Enhancer	TF binding region CpG island lncRNA miRNA	5 gene(s)	inside rSNPs	diseases
42	nsv878669	chr4:9551094-9794724	Active TSS Weak transcription Enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA	16 gene(s)	inside rSNPs	diseases
43	nsv878670	chr4:9563294-9651413	Enhancers Strong transcription Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers	TF binding region CpG island	3 gene(s)	inside rSNPs	diseases
44	esv1830672	chr4:9572407-9681650	Weak transcription Enhancers Bivalent Enhancer Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:49 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:9585600-9605400	Weak transcription	Fetal Brain Male	brain
2	chr4:9595200-9605600	Weak transcription	Ovary	ovary
3	chr4:9597600-9605000	Weak transcription	Stomach Mucosa	stomach
4	chr4:9598800-9605400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
5	chr4:9601000-9605400	Weak transcription	Colon Smooth Muscle	Colon
6	chr4:9602000-9605400	Enhancers	Fetal Thymus	thymus
7	chr4:9602200-9604600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
8	chr4:9602200-9606200	Enhancers	HUES48 Cell Line	embryonic stem cell
9	chr4:9602600-9605400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
10	chr4:9602800-9604400	Enhancers	Primary hematopoietic stem cells short term culture	blood
11	chr4:9602800-9605800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
12	chr4:9603000-9604400	Enhancers	iPS-15b Cell Line	embryonic stem cell
13	chr4:9603000-9604400	Enhancers	Primary hematopoietic stem cells	blood
14	chr4:9603000-9606400	Enhancers	iPS-18 Cell Line	embryonic stem cell
15	chr4:9603200-9604400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
16	chr4:9603200-9604400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
17	chr4:9603200-9604800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr4:9603400-9604400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
19	chr4:9603400-9604400	Enhancers	H1 Cell Line	embryonic stem cell
20	chr4:9603400-9604400	Enhancers	Fetal Lung	lung
21	chr4:9603400-9604400	Enhancers	Small Intestine	intestine
22	chr4:9603400-9604400	Enhancers	Thymus	Thymus
23	chr4:9603400-9605400	Enhancers	Primary T cells fromperipheralblood	blood
24	chr4:9603400-9605400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
25	chr4:9603600-9604400	Enhancers	ES-I3 Cell Line	embryonic stem cell
26	chr4:9603600-9605400	Weak transcription	Rectal Mucosa Donor 29	rectum
27	chr4:9603600-9607800	Enhancers	HUES6 Cell Line	embryonic stem cell
28	chr4:9603800-9604400	Enhancers	Primary T killer memory cells from peripheral blood	blood
29	chr4:9603800-9604600	Enhancers	Primary T helper cells fromperipheralblood	blood
30	chr4:9603800-9605400	Weak transcription	Primary T cells from cord blood	blood
31	chr4:9603800-9605400	Active TSS	Duodenum Mucosa	Duodenum
32	chr4:9603800-9605600	Enhancers	iPS-20b Cell Line	embryonic stem cell
33	chr4:9603800-9607200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
34	chr4:9604000-9604400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
35	chr4:9604000-9604400	Active TSS	Colonic Mucosa	Colon
36	chr4:9604000-9604400	Flanking Active TSS	Fetal Intestine Large	intestine
37	chr4:9604000-9604600	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
38	chr4:9604000-9605000	Weak transcription	Primary T helper cells PMA-I stimulated	--
39	chr4:9604000-9605400	Weak transcription	Rectal Smooth Muscle	rectum
40	chr4:9604200-9604400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
41	chr4:9604200-9604400	Enhancers	H9 Cell Line	embryonic stem cell
42	chr4:9604200-9604400	Bivalent Enhancer	Fetal Muscle Trunk	muscle
43	chr4:9604200-9604600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
44	chr4:9604200-9604800	Enhancers	HUES64 Cell Line	embryonic stem cell
45	chr4:9604200-9605400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
46	chr4:9604200-9605400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
47	chr4:9604200-9605400	Weak transcription	Fetal Kidney	kidney
48	chr4:9604200-9605400	Weak transcription	Sigmoid Colon	Sigmoid Colon
49	chr4:9604200-9606200	Active TSS	Fetal Intestine Small	intestine

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