Variant report

Variant	rs577469855
Chromosome Location	chr7:100492813-100492814
allele	C/T
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	STAT1	chr7:100492516-100492844	GM12878	blood:	n/a	n/a
2	HDAC2	chr7:100492683-100493016	K562	blood:	n/a	n/a
3	CTCF	chr7:100492350-100492844	MCF-7	breast:	n/a	chr7:100492576-100492594 chr7:100492813-100492822 chr7:100492579-100492592
4	RAD21	chr7:100492293-100492869	H1-hESC	embryonic stem cell:	n/a	chr7:100492577-100492596 chr7:100492582-100492594
5	CTCF	chr7:100492793-100492866	GM19240	blood:	n/a	chr7:100492813-100492822
6	RAD21	chr7:100492240-100492985	H1-hESC	embryonic stem cell:	n/a	chr7:100492577-100492596 chr7:100492582-100492594
7	ELF1	chr7:100492491-100492911	GM12878	blood:	n/a	chr7:100492571-100492580 chr7:100492574-100492583 chr7:100492740-100492752
8	RAD21	chr7:100492293-100493033	MCF-7	breast:	n/a	chr7:100492577-100492596 chr7:100492582-100492594
9	SMC3	chr7:100491838-100492873	GM12878	blood:	n/a	chr7:100492630-100492640
10	RAD21	chr7:100492354-100492819	A549	lung:	n/a	chr7:100492577-100492596 chr7:100492582-100492594
11	CTCF	chr7:100491721-100493493	SK-N-SH	brain:	n/a	chr7:100492576-100492594 chr7:100492984-100492997 chr7:100493289-100493302 chr7:100492813-100492822 chr7:100492579-100492592
12	JUN	chr7:100492328-100492858	K562	blood:	n/a	n/a
13	EP300	chr7:100492775-100492959	K562	blood:	n/a	chr7:100492862-100492878 chr7:100492866-100492882
14	ZBTB7A	chr7:100492302-100493511	K562	blood:	n/a	n/a
15	SIN3AK20	chr7:100492314-100492993	PANC-1	pancreas:	n/a	n/a
16	CTCF	chr7:100492406-100492894	GM12892	blood:	n/a	chr7:100492576-100492594 chr7:100492813-100492822 chr7:100492579-100492592
17	ZEB1	chr7:100492470-100492868	GM12878	blood:	n/a	n/a
18	HMGN3	chr7:100492415-100495041	K562	blood:	n/a	n/a
19	ZBTB7A	chr7:100492182-100495231	K562	blood:	n/a	n/a
20	EBF1	chr7:100492662-100492879	GM12878	blood:	n/a	n/a
21	CTCF	chr7:100492424-100492813	H1-hESC	embryonic stem cell:	n/a	chr7:100492576-100492594 chr7:100492579-100492592
22	ELF1	chr7:100492338-100493495	GM12878	blood:	n/a	chr7:100493197-100493209 chr7:100492571-100492580 chr7:100493216-100493228 chr7:100492574-100492583 chr7:100492740-100492752 chr7:100493292-100493304
23	UBTF	chr7:100492437-100494200	K562	blood:	n/a	n/a
24	RAD21	chr7:100492386-100492849	H1-hESC	embryonic stem cell:	n/a	chr7:100492577-100492596 chr7:100492582-100492594
25	POLR2A	chr7:100492412-100492845	H1-neurons	neurons:	n/a	n/a
26	RAD21	chr7:100492253-100493054	HCT-116	colon:	n/a	chr7:100492577-100492596 chr7:100492582-100492594
27	RAD21	chr7:100492316-100492946	MCF-7	breast:	n/a	chr7:100492577-100492596 chr7:100492582-100492594
28	FOXM1	chr7:100492442-100492948	GM12878	blood:	n/a	n/a
29	HDAC2	chr7:100492533-100492921	K562	blood:	n/a	n/a
30	TBL1XR1	chr7:100492540-100492938	GM12878	blood:	n/a	n/a
31	ZBTB7A	chr7:100492745-100492892	HepG2	liver:	n/a	n/a
32	CTCF	chr7:100492780-100492930	GM12875	blood:	n/a	chr7:100492813-100492822
33	ELF1	chr7:100492356-100492919	K562	blood:	n/a	chr7:100492571-100492580 chr7:100492574-100492583 chr7:100492740-100492752
34	MTA3	chr7:100492589-100493167	GM12878	blood:	n/a	n/a
35	REST	chr7:100492438-100493008	K562	blood:	n/a	chr7:100492875-100492888
36	RELA	chr7:100492534-100492965	GM15510	blood:	n/a	n/a
37	MAZ	chr7:100492409-100493040	K562	blood:	n/a	n/a
38	CTCF	chr7:100492305-100492855	HCT-116	colon:	n/a	chr7:100492576-100492594 chr7:100492813-100492822 chr7:100492579-100492592
39	ELF1	chr7:100492497-100492943	K562	blood:	n/a	chr7:100492571-100492580 chr7:100492574-100492583 chr7:100492740-100492752
40	HDAC2	chr7:100492345-100495320	MCF-7	breast:	n/a	n/a
41	RAD21	chr7:100492286-100492898	ECC-1	luminal epithelium:	n/a	chr7:100492577-100492596 chr7:100492582-100492594
42	EGR1	chr7:100492691-100494069	K562	blood:	n/a	chr7:100493231-100493244 chr7:100493232-100493243 chr7:100493233-100493243 chr7:100493231-100493244 chr7:100493231-100493245 chr7:100492856-100492869 chr7:100493233-100493243 chr7:100493508-100493522 chr7:100493531-100493545 chr7:100493227-100493249 chr7:100492860-100492870 chr7:100493231-100493244 chr7:100492743-100492756 chr7:100493234-100493243 chr7:100493581-100493595 chr7:100493232-100493243 chr7:100493562-100493576 chr7:100493233-100493242 chr7:100493256-100493266 chr7:100493512-100493522
43	NR2F2	chr7:100492343-100492817	K562	blood:	n/a	n/a
44	UBTF	chr7:100492487-100493492	K562	blood:	n/a	n/a
45	RAD21	chr7:100492301-100493066	HCT-116	colon:	n/a	chr7:100492577-100492596 chr7:100492582-100492594
46	SIN3A	chr7:100492426-100492850	H1-hESC	embryonic stem cell:	n/a	chr7:100492487-100492500
47	CCNT2	chr7:100492094-100495029	K562	blood:	n/a	chr7:100492742-100492751
48	MAZ	chr7:100492395-100493417	IMR90	lung:	n/a	n/a
49	RELA	chr7:100492522-100493017	GM18951	blood:	n/a	n/a
50	CTCF	chr7:100492029-100493295	A549	lung:	n/a	chr7:100492576-100492594 chr7:100492984-100492997 chr7:100492813-100492822 chr7:100492579-100492592

No.	Distal block	Cell Line	Cell type
1	chr7:100491420..100497264-chr7:100607951..100612175,9	K562	blood:
2	chr7:100492296..100493068-chr7:100887259..100887881,3	MCF-7	breast:
3	chr7:100491227..100493354-chr7:100886184..100889152,2	K562	blood:
4	chr7:100491799..100497264-chr7:100607837..100612175,9	K562	blood:
5	chr7:100492615..100493493-chr7:100609306..100609962,2	MCF-7	breast:
6	chr7:100492151..100493007-chr7:100781451..100782108,2	MCF-7	breast:
7	chr7:100492126..100493072-chr7:100720609..100721480,6	MCF-7	breast:
8	chr7:100492534..100493288-chr7:100720555..100721076,2	K562	blood:
9	chr7:100492344..100495062-chr7:100726871..100729209,3	MCF-7	breast:
10	chr7:100492173..100493049-chr7:100701899..100703390,5	K562	blood:
11	chr7:100491373..100494455-chr7:100609680..100612292,3	MCF-7	breast:
12	chr7:100491924..100495059-chr7:100886100..100889819,5	MCF-7	breast:
13	chr7:100492733..100496183-chr7:100699112..100703676,5	MCF-7	breast:
14	chr7:100491458..100494589-chr7:100859109..100862606,4	MCF-7	breast:

Variant related genes	Relation type
ACHE	TF binding region
ENSG00000106397	Chromatin interaction
ENSG00000214253	Chromatin interaction
ENSG00000106400	Chromatin interaction
ENSG00000222636	Chromatin interaction
ENSG00000169871	Chromatin interaction
ENSG00000169894	Chromatin interaction
ENSG00000225946	Chromatin interaction

Extended variants
information (count: 31 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:31 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv1829095	chr7:99814675-100494084	Bivalent Enhancer Active TSS Weak transcription Strong transcription Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	393 gene(s)	inside rSNPs	diseases
2	nsv1020837	chr7:100313122-100508635	Genic enhancers Weak transcription Active TSS Strong transcription Enhancers Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	92 gene(s)	inside rSNPs	diseases
3	esv1832517	chr7:100355490-100749246	Strong transcription Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Enhancers Weak transcription 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 miRNA target site	96 gene(s)	inside rSNPs	diseases
4	esv2758125	chr7:100355490-100749246	Genic enhancers Weak transcription Transcr. at gene 5' and 3' Bivalent Enhancer Active TSS ZNF genes & repeats Enhancers Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	96 gene(s)	inside rSNPs	diseases
5	esv2759547	chr7:100355490-100749246	Active TSS Weak transcription Genic enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	96 gene(s)	inside rSNPs	diseases
6	nsv464647	chr7:100374087-100497131	Flanking Active TSS Strong transcription Bivalent/Poised TSS Genic enhancers Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	90 gene(s)	inside rSNPs	diseases
7	nsv607965	chr7:100374087-100497131	Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers Active TSS Flanking Active TSS Weak transcription Strong transcription Enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	90 gene(s)	inside rSNPs	diseases
8	nsv1032673	chr7:100382250-100606794	Enhancers Weak transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	92 gene(s)	inside rSNPs	diseases
9	nsv888799	chr7:100406144-100497131	Enhancers Bivalent Enhancer Active TSS Weak transcription Genic enhancers Strong transcription Flanking Active TSS 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 miRNA miRNA target site	89 gene(s)	inside rSNPs	diseases
10	nsv888801	chr7:100416250-100497131	Active TSS Enhancers Genic enhancers Weak transcription Transcr. at gene 5' and 3' Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	89 gene(s)	inside rSNPs	diseases
11	nsv464648	chr7:100422156-100518458	Enhancers Strong transcription Genic enhancers Bivalent/Poised TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	90 gene(s)	inside rSNPs	diseases
12	nsv607966	chr7:100422156-100518458	Enhancers Active TSS Weak transcription Genic enhancers Flanking Active TSS Strong transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	90 gene(s)	inside rSNPs	diseases
13	nsv831073	chr7:100425659-100544888	Bivalent Enhancer Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Strong transcription Active TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	88 gene(s)	inside rSNPs	diseases
14	nsv888802	chr7:100484917-100495530	Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Enhancers Genic enhancers Flanking Bivalent TSS/Enh Active TSS Transcr. at gene 5' and 3' Strong transcription Weak transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
15	nsv607968	chr7:100486035-100492896	Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh Active TSS Enhancers Bivalent Enhancer Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region miRNA target site	39 gene(s)	inside rSNPs	diseases
16	nsv888803	chr7:100486656-100497131	Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent Enhancer Weak transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Enhancers Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	39 gene(s)	inside rSNPs	diseases
17	nsv888804	chr7:100486754-100494202	Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	39 gene(s)	inside rSNPs	diseases
18	nsv888805	chr7:100486754-100498057	Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	39 gene(s)	inside rSNPs	diseases
19	nsv482110	chr7:100487616-100493541	Weak transcription Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region	36 gene(s)	inside rSNPs	diseases
20	nsv888806	chr7:100488407-100495530	Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Active TSS Genic enhancers Bivalent/Poised TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases
21	nsv888807	chr7:100490077-100498057	Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Genic enhancers Active TSS Weak transcription Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
22	nsv888808	chr7:100490981-100498057	Bivalent Enhancer Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
23	nsv888809	chr7:100491451-100495530	Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
24	nsv888810	chr7:100492127-100495530	Weak transcription Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Enhancers Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
25	nsv888811	chr7:100492127-100497131	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Genic enhancers Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
26	nsv888812	chr7:100492127-100498057	Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Enhancers Weak transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
27	nsv888813	chr7:100492322-100495530	Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Enhancers Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
28	nsv607969	chr7:100492357-100493998	Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Active TSS Enhancers Weak transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
29	nsv888814	chr7:100492357-100495530	Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Enhancers Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
30	nsv888815	chr7:100492357-100497131	Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Bivalent/Poised TSS Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
31	nsv607970	chr7:100492493-100494949	Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Active TSS Enhancers Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:100491200-100493600	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
2	chr7:100491600-100493400	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin02	Skin
3	chr7:100491800-100493600	Active TSS	H9 Cell Line	embryonic stem cell
4	chr7:100491800-100493600	Active TSS	HSMM	muscle
5	chr7:100491800-100493800	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
6	chr7:100491800-100495000	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
7	chr7:100492000-100493200	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
8	chr7:100492000-100493400	Flanking Bivalent TSS/Enh	Foreskin Keratinocyte Primary Cells skin02	Skin
9	chr7:100492000-100493600	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
10	chr7:100492000-100493600	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
11	chr7:100492000-100493600	Flanking Bivalent TSS/Enh	Foreskin Keratinocyte Primary Cells skin03	Skin
12	chr7:100492000-100493800	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
13	chr7:100492000-100493800	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
14	chr7:100492000-100494000	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin01	Skin
15	chr7:100492200-100493000	Active TSS	HUES48 Cell Line	embryonic stem cell
16	chr7:100492200-100493000	Flanking Bivalent TSS/Enh	Fetal Stomach	stomach
17	chr7:100492200-100493000	Weak transcription	Gastric	stomach
18	chr7:100492200-100493000	Flanking Active TSS	Placenta Amnion	Placenta Amnion
19	chr7:100492200-100493000	Active TSS	GM12878-XiMat	blood
20	chr7:100492200-100493200	Active TSS	Breast Myoepithelial Primary Cells	Breast
21	chr7:100492200-100493400	Flanking Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
22	chr7:100492200-100493400	Flanking Bivalent TSS/Enh	Colonic Mucosa	Colon
23	chr7:100492200-100493600	Active TSS	iPS-15b Cell Line	embryonic stem cell
24	chr7:100492200-100493600	Flanking Active TSS	Primary hematopoietic stem cells	blood
25	chr7:100492200-100493600	Bivalent/Poised TSS	Skeletal Muscle Male	skeletal muscle
26	chr7:100492200-100493600	Active TSS	Skeletal Muscle Female	skeletal muscle
27	chr7:100492200-100493800	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
28	chr7:100492200-100493800	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
29	chr7:100492200-100493800	Active TSS	HepG2	liver
30	chr7:100492200-100494200	Bivalent Enhancer	Spleen	Spleen
31	chr7:100492200-100495000	Bivalent/Poised TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
32	chr7:100492400-100493000	Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
33	chr7:100492400-100493000	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
34	chr7:100492400-100493000	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
35	chr7:100492400-100493000	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
36	chr7:100492400-100493000	Enhancers	Pancreas	Pancrea
37	chr7:100492400-100493000	Active TSS	Rectal Mucosa Donor 31	rectum
38	chr7:100492400-100493200	Bivalent Enhancer	Primary monocytes fromperipheralblood	blood
39	chr7:100492400-100493200	Flanking Bivalent TSS/Enh	Primary T helper naive cells fromperipheralblood	blood
40	chr7:100492400-100493200	Flanking Bivalent TSS/Enh	Fetal Adrenal Gland	Adrenal Gland
41	chr7:100492400-100493200	Flanking Bivalent TSS/Enh	Fetal Intestine Large	intestine
42	chr7:100492400-100493200	Flanking Bivalent TSS/Enh	Fetal Muscle Trunk	muscle
43	chr7:100492400-100493400	Flanking Bivalent TSS/Enh	Primary T helper cells PMA-I stimulated	--
44	chr7:100492400-100493400	Flanking Bivalent TSS/Enh	Primary T helper cells fromperipheralblood	blood
45	chr7:100492400-100493400	Flanking Bivalent TSS/Enh	Primary T regulatory cells fromperipheralblood	blood
46	chr7:100492400-100493400	Flanking Bivalent TSS/Enh	Primary T cells effector/memory enriched fromperipheralblood	blood
47	chr7:100492400-100493400	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
48	chr7:100492400-100493600	Bivalent/Poised TSS	H1 Cell Line	embryonic stem cell
49	chr7:100492400-100493600	Bivalent/Poised TSS	Duodenum Mucosa	Duodenum
50	chr7:100492400-100493600	Bivalent Enhancer	Fetal Brain Male	brain

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