Variant report

Variant	rs56887572
Chromosome Location	chr6:143398896-143398897
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:18 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:143382600-143426800	Weak transcription	Ovary	ovary
2	chr6:143384200-143407400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
3	chr6:143384200-143407600	Weak transcription	Psoas Muscle	Psoas
4	chr6:143386000-143403800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr6:143386400-143431800	Weak transcription	NHEK	skin
6	chr6:143389600-143400000	Weak transcription	HUES48 Cell Line	embryonic stem cell
7	chr6:143389600-143437000	Weak transcription	HSMM	muscle
8	chr6:143389800-143400000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
9	chr6:143389800-143418800	Weak transcription	Osteobl	bone
10	chr6:143395800-143432200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
11	chr6:143396600-143402200	Enhancers	Liver	Liver
12	chr6:143396800-143399400	Weak transcription	Small Intestine	intestine
13	chr6:143396800-143400000	Weak transcription	Fetal Intestine Large	intestine
14	chr6:143397400-143431600	Weak transcription	HMEC	breast
15	chr6:143397600-143399400	Weak transcription	HepG2	liver
16	chr6:143397600-143400000	Weak transcription	Fetal Intestine Small	intestine
17	chr6:143398000-143408000	Weak transcription	Left Ventricle	heart
18	chr6:143398800-143404000	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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